A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726806



Internal ID150472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36956677..36957799hg38UCSC Ensembl
chr21:38328977..38330099hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg381123
hg191123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146601
Supporting Variants
Samples
Known GenesHLCS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726806
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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